CrawlJobs Logo

Pharmaceutical packaging

https://www.randstad.com Logo

Randstad

Location Icon

Location:
Canada , Mississauga

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

18.00 CAD / Hour

Job Description:

Pharmaceutical light packaging available in Mississauga. Shift available: 7:00AM-3:15PM. Duration: End date unknown.

Job Responsibility:

  • Packaging
  • Sorting
  • Inspection
  • Ticketing
  • Labelling
  • Must have attention to detail
  • Other warehouse duties may be expected

Requirements:

  • Must have previous packaging experience (6 months)
  • Must be able to pass a GMP test
  • Safety shoes are a MUST
  • Safety glasses
  • No jewelry, no make up, no nail polish or fake nails are allowed inside the facility
What we offer:
  • Long term work
  • Clean and bright warehouse to work in
  • Buses available
  • Friendly staff to work with
  • Client will provide a lab coat and hair/beard net

Additional Information:

Job Posted:
December 25, 2025

Expiration:
February 11, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Pharmaceutical packaging

Pharmaceutical packaging night

Pharmaceutical light packaging available in Mississauga. Shift: 11:00PM- 7:00AM....
Location
Location
Canada , Mississauga
Salary
Salary:
18.00 CAD / Hour
https://www.randstad.com Logo
Randstad
Expiration Date
February 11, 2026
Flip Icon
Requirements
Requirements
  • Must have previous packaging experience (6 months)
  • Must be able to pass a GMP test
  • Safety shoes are a MUST
  • Safety glasses
  • No jewelry, no make up, no nail polish or fake nails are allowed inside the facility
Job Responsibility
Job Responsibility
  • Packaging
  • Sorting
  • Inspection
  • Ticketing
  • Labelling
  • Must have attention to detail
  • Other warehouse duties may be expected
What we offer
What we offer
  • Long term work
  • Clean and bright warehouse to work in
  • Buses available
  • Friendly staff to work with
  • Client will provide a lab coat and hair/beard net
  • Fulltime
!
Read More
Arrow Right

Principal, Packaging Engineering

Lead all aspects of packaging process development, qualification, validation, la...
Location
Location
United States
Salary
Salary:
180000.00 - 240000.00 USD / Year
loyal.com Logo
Loyal
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s, Master’s, or PhD in Packaging Engineering, Chemical Engineering, Mechanical Engineering, Materials Science, or a related field
  • 10+ years of experience in pharmaceutical or biopharmaceutical packaging engineering, with significant experience supporting commercial or late-stage OSD products
  • Deep expertise in small molecule, oral solid dosage packaging, including bottling, blister packaging, labeling, serialization, and container–closure systems
  • Proven success leading packaging process development, scale-up, qualification, and validation (IQ/OQ/PQ)
  • Strong experience with CDMO/CMO selection, technical transfer, and day-to-day management for packaging operations
  • Experience supporting commercial packaging operations, including launch readiness and ongoing supply
  • Demonstrated ability to author packaging sections of regulatory submissions (e.g., Module 3) and respond to packaging-related regulatory questions
  • Strong understanding of global packaging regulatory expectations (FDA, EMA, ICH), including CR/SF requirements and serialization/traceability standards
  • Experience with packaging component qualification, compatibility studies, and packaging-related stability requirements
  • Experience supporting or participating in pre-approval inspections (PAIs) related to packaging
Job Responsibility
Job Responsibility
  • Lead packaging process development, scale-up, and optimization for OSD drug products
  • Drive CDMO/CMO selection, including technical evaluations, audits, contracting, and governance for packaging operations
  • Develop and refine packaging processes, ensuring robustness, manufacturability, and compliance with regulatory and product requirements
  • Lead packaging qualification and validation (IQ/OQ/PQ) for launch and commercial readiness
  • Oversee packaging launch readiness, including artwork, labeling, serialization, child-resistant/senior-friendly requirements, packaging components, and distribution-related packaging needs
  • Establish and oversee commercial packaging operations, ensuring efficiency, compliance, and long-term supply continuity
  • Author and contribute to packaging-related sections of regulatory submissions (Module 3), including container closure system documentation, packaging process descriptions, and responses to regulatory queries
  • Support or participate in PAIs and other regulatory interactions related to packaging
  • Conduct and oversee packaging component qualification, compatibility studies, and packaging-related stability evaluations
  • Troubleshoot packaging issues, conduct root-cause investigations, and lead CAPAs
What we offer
What we offer
  • Full-coverage health insurance — medical, dental and vision — for you and your dependents
  • $1,000 home office equipment stipend
  • $1,200/year learning budget for books, courses, etc.
  • $250/month wellness budget for gym, cleaners, spa, food, etc.
  • All 3-day weekends are turned into 4-day weekends
  • Unlimited vacation and paid holidays
  • Paw-ternity leave — adopt a dog and get a day off with your new family member
  • Competitive salary
  • Company equity options grant for new hires
  • Fulltime
Read More
Arrow Right

Packaging Technician

Reporting to Packaging Team Lead, the Packaging Technician is responsible for th...
Location
Location
Ireland , Cork
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Previous experience in a highly regulated operating environment such as the biologics, pharmaceutical or medical device sectors is desirable though not essential
  • Previous packaging experience will be considered advantageous
  • Demonstrated experience (2+ years) of operating in a team environment (professional) is required
  • Must be conscientious and possess strong teamwork and interpersonal skills
  • Strong communication and problem-solving skills are highly valued
Job Responsibility
Job Responsibility
  • Work as part of a team of Packaging Technicians to complete the packaging of Finished Produce for onward distribution
  • Detailed batch record keeping which is accurate, complete, legible and in accordance with cGMP requirements
  • Identify issues on the line and alert the Packaging Equipment Technician
  • Provide support to the Packaging Equipment Technician to help resolve issues on the line as required
  • Carry out transactions on SAP as required
  • Ensure the Packaging area is Inspection Ready at all times
  • Participate in Regulatory Inspections
  • Assist with writing, review and revision of packing documentation as necessary (e.g. batch records, standard operation procedure etc)
  • Demonstrate commitment to a high level of safety awareness with the Packaging Operations Team
  • Proactively support continuous improvement and lead initiatives with the Packaging Suite
  • Fulltime
Read More
Arrow Right

Quality Assurance Packaging Specialist

This position within the QA department provides Quality oversight, support and k...
Location
Location
Ireland , Cork
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree or 3rd level qualification (Science, Quality)
  • Demonstrated experience in packaging as the Quality contact for the area
  • Relevant experience (5yrs +) working in a Quality function in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the other requirements of the role
  • Demonstrates good knowledge of FDA / EMEA regulations/standards and quality systems
  • Demonstrated ability to work independently and fully realize improvement initiatives with a moderate level of guidance
  • Demonstrated ability to work and succeed within teams as well as leading small project teams while maintaining and strengthening trust relationships with people on all levels
  • Strong organizational skills, including ability to follow assignments through to completion
  • Proficiency in PC skills such as Excel, Word, PowerPoint
  • Proven decision making capability with full accountability and responsibility
  • Demonstrated coaching skills
Job Responsibility
Job Responsibility
  • Provide Quality input and guidance to ensure packaging of high quality products in compliance with current Good Manufacturing Practices (GMPs)
  • Provide Quality direction and oversight of the development of new and existing processes in the packaging area to meet customer needs
  • Exercise judgment to determine appropriate action, ensuring proper escalation when non-conformances are identified as per applicable procedures for compliance, escalation and corrections within the packaging area of operations
  • Provide Quality input to Change Control/Deviations ensuring scope of record is clear and implementation activities are robust and timely
  • Review and approval of NCs and associated CAPAs for closure ensuring compliance with appropriate documentation, whilst ensuring that CAPA actions address root cause and implementation plan dates are achievable
  • Participates within inter-departmental and cross-functional teams, with direct interface with Manufacturing, Supply & Distribution, Maintenance, Metrology and Quality Control employees to immediately address issues and questions in real time to help ensure timeline are achieved to meet customer requirements
  • Minimising impact to packaging operations on site
  • Prioritizes tasks to ensure the critical tasks are completed on time and meet requirements
  • Review and release inputs for use in manufacturing as required
  • Write, review and approve Standard Operating Procedures in accordance with BioMarin Policies
  • Fulltime
Read More
Arrow Right

Service Engineer

A classic Field Service Engineer role working for a well established worldwide m...
Location
Location
United Kingdom , Birmingham
Salary
Salary:
50000.00 GBP / Year
https://www.wallacehind.com Logo
Wallace Hind
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • You MUST have a proven track record as a Field Service Engineer or as a Factory Maintenance Engineer working within the pharmaceutical or food markets
  • You will ideally have hands on experience of working upon packaging and/or process machinery
  • You will also be a qualified Multi-skilled Engineer
  • You will be willing and able to travel and stay away as required above.
Job Responsibility
Job Responsibility
  • Installation and commissioning of machinery
  • Repairs, modification, and upgrades of existing machinery
  • Travel and stay away from home worldwide for circa 30 weeks a year
  • Training and induction at the UK factory.
What we offer
What we offer
  • Circa £7,500 travel allowance
  • All expenses covered whilst working abroad
  • 7.5% pension
  • Full induction and product training
  • Paid overtime door to door.
  • Fulltime
Read More
Arrow Right

Senior Manufacturing Process Technician

In this role you will be operating an automated and innovative manufacturing equ...
Location
Location
United States , New Albany
Salary
Salary:
65840.00 - 82251.00 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High school diploma and 2 years of technical experience in Pharmaceutical, Manufacturing, or Packaging environment
  • Associate’s degree and 6 months of technical experience in Pharmaceutical, Manufacturing, or Packaging environment
  • Ability to follow written procedures
  • Ability to stand or sit for extended periods of time
  • Ability to lift 35 pounds
  • Capability to diagnose malfunctions and perform equipment setup
  • Educational Background in Mechanical, Electronic Engineering Technology or Industrial Mechanics
  • Working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment
  • Ability to use computer systems to support the material inventory system (SAP transactions) and electronic batch records
  • Excellent attention to detail, good organization, and capable of working independently
Job Responsibility
Job Responsibility
  • Perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency
  • Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment
  • Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions
  • Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)
  • Assist as training resource on manufacturing tasks and equipment use
  • Use human machine interfaces (HMIs) to identify alarms and correct line stoppages
  • Ensures components and products are available for a continuous operation
  • Carries out equipment inspections and generates emergency, corrective, or preventative work orders
  • Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes
  • Partner with cross-functional teams to help drive improvement opportunities
What we offer
What we offer
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models, including remote and hybrid work arrangements, where possible
  • Fulltime
Read More
Arrow Right

Pharmacy Technician I

Assists Pharmacist in processing and compounding prescriptions and other drug or...
Location
Location
United States , Tucson
Salary
Salary:
Not provided
tmcaz.com Logo
Tucson Medical Center
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High school diploma or general education degree (GED), or an equivalent combination of relevant education and experience
  • Licensed by the Arizona State Board of Pharmacy as Technician Trainee
  • Pharmacy Technician licensure obtained within one year of hire
  • Heartsaver CPR (HSCPR or HSFACPR) or Basic Life Support (BLS) certification required
  • Knowledge of pharmaceutical practices and procedures and regulations involving the administering of medications
  • Knowledge of medicine terminology
  • Skill in compounding and processing prescriptions
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
  • Ability to complete routine reports and correspondence
  • Ability to listen and accurately interpret others’ communication or instructions to take appropriate action
Job Responsibility
Job Responsibility
  • Assists Pharmacist in processing and compounding prescriptions and other drug orders
  • Pulls prescribed medication from shelf
  • Enters medication charges into the computer
  • Restocks pharmacy automation shelves
  • Handles telephone inquiries
  • Assists pharmacists as directed, including filling orders and preparing labels
  • Clarifies orders for all types of medications
  • Documents pertinent information in a clear, complete, concise and organized manner
  • Complies with Federal and State statutes, rules and regulations regarding the practice of pharmacy
  • Prepares and makes deliveries to patient care areas and ancillary units
  • Fulltime
Read More
Arrow Right

Principal Engineer – Nutrition Containers

This is a high-impact role where your technical expertise and leadership will di...
Location
Location
Belgium , Braine-l'Alleud
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in engineering or a related field
  • 5–10 years of experience in product design, preferably in medical devices or pharmaceutical packaging
  • Strong understanding of cross-disciplinary engineering practices
  • Proven ability to lead projects and influence stakeholders
  • Experience in risk management and design validation
  • People leadership skills with a fair and ethical approach to team development
  • Excellent communication and problem-solving abilities
Job Responsibility
Job Responsibility
  • Lead Engineering Projects: Drive the design and development of containers, from concept through validation, ensuring compliance with regulatory and quality standards
  • Technical Leadership: Act as a subject matter expert in container design, risk project management, and verification/validation activities
  • Problem Solving & Innovation: Apply advanced engineering principles to solve complex design challenges and lead root cause investigations (DMAIC approach)
  • Project Management: Independently manage sub-projects within cross-functional teams, ensuring timely delivery and alignment with business goals
  • Team Development: Manage and mentor a small team of engineers based in Malta & Belgium, fostering growth, collaboration, and technical excellence
  • Cross-Functional Collaboration: Work closely with R&D, Quality, Regulatory, and Manufacturing teams across Baxter’s global network
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Opportunities for global career growth
  • Competitive benefits
  • Flexibility to support a healthy work-life balance
Read More
Arrow Right